Persistent renal enhancement after intra-arterial versus intravenous iodixanol administration

Abstract Purpose To examine the clinical significance of persistent renal enhancement after iodixanol administration. Methods We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial ( n = 99) or intravenous ( n = 6...

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Published inEuropean journal of radiology Vol. 80; no. 2; pp. 378 - 386
Main Authors Chou, Shinn-Huey, Wang, Zhen J, Kuo, Jonathan, Cabarrus, Miguel, Fu, Yanjun, Aslam, Rizwan, Yee, Judy, Zimmet, Jeffrey M, Shunk, Kendrick, Elicker, Brett, Yeh, Benjamin M
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Published Amsterdam Elsevier Ireland Ltd 01.11.2011
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Abstract Abstract Purpose To examine the clinical significance of persistent renal enhancement after iodixanol administration. Methods We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial ( n = 99) or intravenous ( n = 67) iodixanol. Renal attenuation was measured for each non-enhanced CT scan. Persistent renal enhancement was defined as CT attenuation >55 Hounsfield units (HU). Contrast-induced nephropathy (CIN) was defined as a rise in serum creatinine >0.5 mg/dL within 5 days after contrast administration. Results While the intensity and frequency of persistent renal enhancement was higher after intra-arterial (mean CT attenuation of 73.7 HU, seen in 54 of 99 patients, or 55%) than intravenous contrast material administration (51.8 HU, seen in 21 of 67, or 31%, p < 0.005), a multivariate regression model showed that the independent predictors of persistent renal enhancement were a shorter time interval until the subsequent non-enhanced CT ( p < 0.001); higher contrast dose ( p < 0.001); higher baseline serum creatinine ( p < 0.01); and older age ( p < 0.05). The route of contrast administration was not a predictor of persistent renal enhancement in this model. Contrast-induced nephropathy was noted in 9 patients who received intra-arterial (9%) versus 3 who received intravenous iodixanol (4%), and was more common in patients with persistent renal enhancement ( p < 0.01). Conclusion Persistent renal enhancement at follow-up non-contrast CT suggests a greater risk for contrast-induced nephropathy, but the increased frequency of striking renal enhancement in patients who received intra-arterial rather than intravenous contrast material also reflects the larger doses of contrast and shorter time to subsequent follow-up CT scanning for such patients.
AbstractList To examine the clinical significance of persistent renal enhancement after iodixanol administration. We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial (n=99) or intravenous (n=67) iodixanol. Renal attenuation was measured for each non-enhanced CT scan. Persistent renal enhancement was defined as CT attenuation>55 Hounsfield units (HU). Contrast-induced nephropathy (CIN) was defined as a rise in serum creatinine>0.5 mg/dL within 5 days after contrast administration. While the intensity and frequency of persistent renal enhancement was higher after intra-arterial (mean CT attenuation of 73.7 HU, seen in 54 of 99 patients, or 55%) than intravenous contrast material administration (51.8 HU, seen in 21 of 67, or 31%, p<0.005), a multivariate regression model showed that the independent predictors of persistent renal enhancement were a shorter time interval until the subsequent non-enhanced CT (p<0.001); higher contrast dose (p<0.001); higher baseline serum creatinine (p<0.01); and older age (p<0.05). The route of contrast administration was not a predictor of persistent renal enhancement in this model. Contrast-induced nephropathy was noted in 9 patients who received intra-arterial (9%) versus 3 who received intravenous iodixanol (4%), and was more common in patients with persistent renal enhancement (p<0.01). Persistent renal enhancement at follow-up non-contrast CT suggests a greater risk for contrast-induced nephropathy, but the increased frequency of striking renal enhancement in patients who received intra-arterial rather than intravenous contrast material also reflects the larger doses of contrast and shorter time to subsequent follow-up CT scanning for such patients.
Abstract Purpose To examine the clinical significance of persistent renal enhancement after iodixanol administration. Methods We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial ( n = 99) or intravenous ( n = 67) iodixanol. Renal attenuation was measured for each non-enhanced CT scan. Persistent renal enhancement was defined as CT attenuation >55 Hounsfield units (HU). Contrast-induced nephropathy (CIN) was defined as a rise in serum creatinine >0.5 mg/dL within 5 days after contrast administration. Results While the intensity and frequency of persistent renal enhancement was higher after intra-arterial (mean CT attenuation of 73.7 HU, seen in 54 of 99 patients, or 55%) than intravenous contrast material administration (51.8 HU, seen in 21 of 67, or 31%, p < 0.005), a multivariate regression model showed that the independent predictors of persistent renal enhancement were a shorter time interval until the subsequent non-enhanced CT ( p < 0.001); higher contrast dose ( p < 0.001); higher baseline serum creatinine ( p < 0.01); and older age ( p < 0.05). The route of contrast administration was not a predictor of persistent renal enhancement in this model. Contrast-induced nephropathy was noted in 9 patients who received intra-arterial (9%) versus 3 who received intravenous iodixanol (4%), and was more common in patients with persistent renal enhancement ( p < 0.01). Conclusion Persistent renal enhancement at follow-up non-contrast CT suggests a greater risk for contrast-induced nephropathy, but the increased frequency of striking renal enhancement in patients who received intra-arterial rather than intravenous contrast material also reflects the larger doses of contrast and shorter time to subsequent follow-up CT scanning for such patients.
To examine the clinical significance of persistent renal enhancement after iodixanol administration. We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial ( n = 99) or intravenous ( n = 67) iodixanol. Renal attenuation was measured for each non-enhanced CT scan. Persistent renal enhancement was defined as CT attenuation >55 Hounsfield units (HU). Contrast-induced nephropathy (CIN) was defined as a rise in serum creatinine >0.5 mg/dL within 5 days after contrast administration. While the intensity and frequency of persistent renal enhancement was higher after intra-arterial (mean CT attenuation of 73.7 HU, seen in 54 of 99 patients, or 55%) than intravenous contrast material administration (51.8 HU, seen in 21 of 67, or 31%, p < 0.005), a multivariate regression model showed that the independent predictors of persistent renal enhancement were a shorter time interval until the subsequent non-enhanced CT ( p < 0.001); higher contrast dose ( p < 0.001); higher baseline serum creatinine ( p < 0.01); and older age ( p < 0.05). The route of contrast administration was not a predictor of persistent renal enhancement in this model. Contrast-induced nephropathy was noted in 9 patients who received intra-arterial (9%) versus 3 who received intravenous iodixanol (4%), and was more common in patients with persistent renal enhancement ( p < 0.01). Persistent renal enhancement at follow-up non-contrast CT suggests a greater risk for contrast-induced nephropathy, but the increased frequency of striking renal enhancement in patients who received intra-arterial rather than intravenous contrast material also reflects the larger doses of contrast and shorter time to subsequent follow-up CT scanning for such patients.
Author Fu, Yanjun
Shunk, Kendrick
Elicker, Brett
Yeh, Benjamin M
Kuo, Jonathan
Zimmet, Jeffrey M
Aslam, Rizwan
Cabarrus, Miguel
Chou, Shinn-Huey
Wang, Zhen J
Yee, Judy
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Issue 2
Keywords CT
Intravenous
Renal
Persistent enhancement
Contrast
Contrast-induced nephropathy
Intra-arterial
Kidney disease
Urinary system disease
Non ionic contrast media
Intravenous administration
Radiodiagnosis
Renal artery
Toxicity
Iodine Organic compounds
Kidney
Nephropathy
Urinary system
Medical imagery
Computerized axial tomography
Iodixanol
Comparative study
Contrast media
Language English
License CC BY 4.0
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
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Snippet Abstract Purpose To examine the clinical significance of persistent renal enhancement after iodixanol administration. Methods We retrospectively studied 166...
To examine the clinical significance of persistent renal enhancement after iodixanol administration. We retrospectively studied 166 consecutive patients who...
SourceID pubmedcentral
crossref
pubmed
pascalfrancis
elsevier
SourceType Open Access Repository
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StartPage 378
SubjectTerms Adult
Age Factors
Aged
Aged, 80 and over
Biological and medical sciences
Contrast
Contrast Media - administration & dosage
Contrast media. Radiopharmaceuticals
Contrast-induced nephropathy
Creatinine - blood
Female
Humans
Injections, Intra-Arterial
Injections, Intravenous
Intra-arterial
Intravenous
Kidney - diagnostic imaging
Kidney Diseases - chemically induced
Kidney Diseases - diagnostic imaging
Male
Medical sciences
Middle Aged
Persistent enhancement
Pharmacology. Drug treatments
Radiology
Regression Analysis
Renal
Retrospective Studies
Tomography, X-Ray Computed
Triiodobenzoic Acids - administration & dosage
Title Persistent renal enhancement after intra-arterial versus intravenous iodixanol administration
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0720048X11002300
https://dx.doi.org/10.1016/j.ejrad.2011.02.044
https://www.ncbi.nlm.nih.gov/pubmed/21470810
https://pubmed.ncbi.nlm.nih.gov/PMC3160516
Volume 80
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